The author of 《Efficient diverse approach for quinoxaline-derived glycosylated and morphinylated analogs》 were Beldi, Razika; Atta, Kamal F.; Aboul-Ela, Sallah; El Ashry, El Sayed H.. And the article was published in Journal of Heterocyclic Chemistry in 2010. Safety of 2-(2-Chloroethoxy)ethyl acetate The author mentioned the following in the article:
Sulfanyl-glycosides have been synthesized by reaction of dimercaptoquinoxaline I (R = H) with aceto-halo sugars in presence of base to give the thioglycosides-derived quinoxalines, e.g. II. Similarly, the acyclic analogs, e.g. I (R = Me), were prepared by coupling of I (R = H) with different acyclo-alkylating agents. The preparation of 3-morpholinyl quinoxalines allowed the synthesis of 3-glycosylsulfanyl-2-morpholinyl quinoxalines as well as the acyclic analogs. Microwave irradiation of the reactants turned out to be preferred over the conventional method for achieving the synthetic goals. This study made an available venue to the synthesis of diverse quinoxaline derivatives The results came from multiple reactions, including the reaction of 2-(2-Chloroethoxy)ethyl acetate(cas: 14258-40-3Safety of 2-(2-Chloroethoxy)ethyl acetate)
2-(2-Chloroethoxy)ethyl acetate(cas: 14258-40-3) belongs to aliphatic hydrocarbons. Aliphatic hydrocarbons belong to the most abundant fraction in crude oil. Aliphatics molecules are linear or branched open-chain structures such as n-alkanes, isoalkanes, cycloalkanes (naphthenes), terpenes and steranes.Safety of 2-(2-Chloroethoxy)ethyl acetate
Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics